Evidence map›Paper›PMID 24850900›Full record

ArticleMolecular cancer research : MCR2014

MIF antagonist (CPSI-1306) protects against UVB-induced squamous cell carcinoma.

Priyadharsini Nagarajan, Kathleen L Tober, Judith A Riggenbach, Donna F Kusewitt, Amy M Lehman, Thais Sielecki, James Pruitt, Abhay R Satoskar, Tatiana M Oberyszyn

Abstract read
In one paragraph

Article in Molecular cancer research : MCR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 27 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Priyadharsini NagarajanDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Kathleen L ToberDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Judith A RiggenbachDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Donna F KusewittDepartment of Molecular Carcinogenesis, Science Park, The University of Texas MD Anderson Cancer Center, Smithville, Texas.
Amy M LehmanCenter for Biostatistics, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Thais SieleckiCytokine PharmaSciences, King of Prussia, Pennsylvania.
James PruittCytokine PharmaSciences, King of Prussia, Pennsylvania.
Abhay R SatoskarDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Tatiana M OberyszynDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio. oberyszyn.1@osu.edu.
The Ohio State University Wexner Medical Center · USEdwards Lifesciences (United States) · USThe University of Texas MD Anderson Cancer Center · US

Funding

Chemopreventition and treatment of non-melanoma skin cancer by targeting MIFR03CA164399 · NCI · OHIO STATE UNIVERSITY · PI SATOSKAR, ABHAY R · 2012 to 2013
$153k
NCI NIH HHS R03 CA164399NCI NIH HHS R03CA164399
6 · The paper itself

Abstract

unlabelledMacrophage migration inhibitory factor (MIF) is a homotrimeric proinflammatory cytokine implicated in chronic inflammatory diseases and malignancies, including cutaneous squamous cell carcinomas (SCC). To determine whether MIF inhibition could reduce UVB light-induced inflammation and squamous carcinogenesis, a small-molecule MIF inhibitor (CPSI-1306) was utilized that disrupts homotrimerization. To examine the effect of CPSI-1306 on acute UVB-induced skin changes, Skh-1 hairless mice were systemically treated with CPSI-1306 for 5 days before UVB exposure. In addition to decreasing skin thickness and myeloperoxidase (MPO) activity, CPSI-1306 pretreatment increased keratinocyte apoptosis and p53 expression, decreased proliferation and phosphohistone variant H2AX (γ-H2AX), and enhanced repair of cyclobutane pyrimidine dimers. To examine the effect of CPSI-1306 on squamous carcinogenesis, mice were exposed to UVB for 10 weeks, followed by CPSI-1306 treatment for 8 weeks. CPSI-1306 dramatically decreased the density of UVB-associated p53 foci in non-tumor-bearing skin while simultaneously decreasing the epidermal Ki67 proliferation index. In addition to slowing the rate of tumor development, CPSI-1306 decreased the average tumor burden per mouse. Although CPSI-1306-treated mice developed only papillomas, nearly a third of papillomas in vehicle-treated mice progressed to microinvasive SCC. Thus, MIF inhibition is a promising strategy for prevention of the deleterious cutaneous effects of acute and chronic UVB exposure. IMPLICATIONS: Macrophage migration inhibitory factor is a viable target for the prevention of UVB-induced cutaneous SSCs.

Indexed as

AnimalsApoptosisCarcinoma, Squamous CellDNA DamageFemaleIntramolecular OxidoreductasesIsoxazolesMacrophage Migration-Inhibitory FactorsMiceMorpholinesNeoplasms, Radiation-InducedSkin NeoplasmsTumor Suppressor Protein p53Ultraviolet RaysCPSI-1306Intramolecular OxidoreductasesIsoxazolesMacrophage Migration-Inhibitory FactorsMIF protein, humanMorpholinesTumor Suppressor Protein p53

Identifiers

PMID24850900
PMCPMC4284200
OpenAlexW2135757311

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.